FDA.reportPublic FDA data

KinetiCream Pain Relieving Topical Analgesic

Manufacturer
Phoenix Bioperformance Products LLC | Pure Source, LLC
Effective date
2026-04-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:52:51

Label at a glance#

ProductKinetiCream Pain Relieving Topical Analgesic
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

For temporary relief of minor aches and pains associated with backache, muscle ache, joint pain, arthritis, bruises and sprains.

Dosage and administration

Shake well prior to using. Apply to area of discomfort. Smooth out and allow to absorb into skin. Do not use more than four times per day.Do not use near eyes. For best results, use immediately after showering.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 2.00%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses:

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains associated with backache, muscle ache, joint pain, arthritis, bruises and sprains.

Warnings:

WARNINGS SECTION

  • For external use only.
  • Avoid contact with eyes.
  • Do not apply to open wounds or damaged skin.
  • If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, consult physician.
  • Do not bandage tightly.

If pregnant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

consult physician prior to use.

Directions.

DOSAGE & ADMINISTRATION SECTION

Shake well prior to using. Apply to area of discomfort. Smooth out and allow to absorb into skin. Do not use more than four times per day.Do not use near eyes. For best results, use immediately after showering.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Juice) Gel, Aqua (Deionized Water), Arnica Montrana Flower Extract, Bromelain, Butyrospermum Parkii (Shea) Butter, C13-14 lsoparaffin, Calophyllum Tacamahaca (Tamanu) Oil, Camellia Sinensis Leaf (Green Tea) Extract, Cetearyl Alcohol, Cetyl Myristoleate, Chondroitin Sulfate, Citric Acid, Citrus Aurantium Bergamia (Bergamot) Oil, Dimethyl Sulfone (MSM), Emu Oil, Ethylhexylglycerin, Glycerin, Glucosamine Sulfate, Glyceryl Stearate SE, Laureth-7, Melia Azadirachta (Neem) Seed Oil, Mentha Piperita (Peppermint) Oil, Papain, Phenoxyethanol, Polyacrylamide, Polysorbate-20, Salix Alba (Willow Bark) Extract, SD-Alcohol 40B, Sesamum lndicum (Sesame) Oil, Stearic Acid, Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate (Vitamin-E), Xanthan Gum.

Questions or Comments?

OTC - QUESTIONS SECTION

Please connect with us on our social media pages or call us at 1.844.KINETIC!

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1102253menthol 2 % Topical CreamPSN1
1102253menthol 20 MG/ML Topical CreamSCD1
1102253menthol 2 % Topical CreamSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130610395562580GTIN-13: 0610395562580
EAN-13: 0610395562580
GTIN-12: 610395562580
UPC-A: 610395562580
GTIN storage (14 digits): 00610395562580		Label.jpg
QR code linkQR Codeqrs.ly/qi3ieqwLabel.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58611-971-00KinetiCream Pain Relieving Topical Analgesic101 mL in 1 BOTTLECREAM1011

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58611-97158611-971-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
BROMELAINU182GP2CF3IACT
SHEA BUTTERK49155WL9YIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
TAMANU OILJT3LVK84A1IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CETEARYL ALCOHOL2DMT128M1SIACT
CETYL MYRISTOLEATE87P8K33Q5XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BERGAMOT OIL39W1PKE3JIIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
EMU OIL344821WD61IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
GLUCOSAMINE SULFATE1FW7WLR731IACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
LAURETH-7Z95S6G8201IACT
AZADIRACHTA INDICA SEED OIL4DKJ9B3K2TIACT
PEPPERMINT OILAV092KU4JHIACT
PAPAINA236A06Y32IACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
SALIX ALBA BARK205MXS71H7IACT
SESAME OILQX10HYY4QVIACT
STEARIC ACID4ELV7Z65APIACT
COCOA BUTTER512OYT1CRRIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
XANTHAN GUMTTV12P4NEEIACT
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
KinetiCream Pain Relieving Topical AnalgesicMENTHOLPhoenix Bioperformance Products LLCbb4c9e73-e62d-4b8c-a16c-b90db1a8b2a72026-04-06WarningsExact identifier
ndc (package): 58611-971-00
ndc (product): 58611-971
ndc11 (package): 58611097100
spl id: 4ecb6ace-0671-e88b-e063-6394a90a379c
spl set id: bb4c9e73-e62d-4b8c-a16c-b90db1a8b2a7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.